美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA080966"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
72162-2237-1 72162-2237 HUMAN PRESCRIPTION DRUG Probenecid Probenecid TABLET, FILM COATED ORAL 20240126 N/A ANDA ANDA080966 Bryant Ranch Prepack PROBENECID 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1)
0527-1367-01 0527-1367 HUMAN PRESCRIPTION DRUG Probenecid Probenecid TABLET, FILM COATED ORAL 19760729 N/A ANDA ANDA080966 Lannett Company, Inc. PROBENECID 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0527-1367-01)
0527-1367-10 0527-1367 HUMAN PRESCRIPTION DRUG Probenecid Probenecid TABLET, FILM COATED ORAL 19760729 N/A ANDA ANDA080966 Lannett Company, Inc. PROBENECID 500 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0527-1367-10)
83008-020-08 83008-020 HUMAN PRESCRIPTION DRUG Probenecid Probenecid TABLET, FILM COATED ORAL 20230524 N/A ANDA ANDA080966 Quality Care Products, LLC PROBENECID 500 mg/1 8 TABLET, FILM COATED in 1 BOTTLE (83008-020-08)
10135-541-01 10135-541 HUMAN PRESCRIPTION DRUG Probenecid Probenecid TABLET, FILM COATED ORAL 19760729 N/A ANDA ANDA080966 Marlex Pharmaceuticals Inc PROBENECID 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (10135-541-01)
10135-541-10 10135-541 HUMAN PRESCRIPTION DRUG Probenecid Probenecid TABLET, FILM COATED ORAL 19760729 N/A ANDA ANDA080966 Marlex Pharmaceuticals Inc PROBENECID 500 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (10135-541-10)
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